| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33001543-33001710 | Common:1; Rare:97; Clinvar (benign):4 | ||||
| chr9:33025093-33025312 | Common:5; Rare:94 | ||||
| chr9:33166774-33166938 | Rare:56; Clinvar:3 | ||||
| chr9:34048876-34048964 | Rare:36 | ||||
| chr9:34329181-34329638 | Common:1; Rare:142 | ||||
| chr9:34620447-34620614 | Common:1; Rare:45 | ||||
| chr9:35103082-35103157 | Common:1; Rare:38 | ||||
| chr9:35103160-35103289 | Rare:30 | ||||
| chr9:35489906-35490130 | Common:2; Rare:64 | ||||
| chr9:35657983-35658342 | Common:6; Rare:269; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):33 | ||||
| chr9:35689813-35690120 | Common:4; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35732088-35732320 | Rare:66 | ||||
| chr9:35732373-35732676 | Common:2; Rare:76 | ||||
| chr9:35749005-35749347 | Common:2; Rare:129 | ||||
| chr9:36036824-36036952 | Common:1; Rare:44 |